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FDA source record Class I Terminated

"Lukai sweetened jujube"; 8.3 ounces; red and yellow packaging; back panel states: "Name: Ejiao dates; Ingredients: a nuclear-free golden jujube, donkey-hide gelatin, sugar, hon...

Recall Date: 2022-12-05 Recalling Firm: Northern Food I/E Inc. Record Ref: F-0212-2023

FINDARECALL QUICK READ

What this record tells you

This FDA record concerns "Lukai sweetened jujube"; 8.3 ounces; red and yellow packaging; back panel states: "Name: Ejiao dates; Ingredients: a nuclear-free golden jujube, donkey-hide gelatin, sugar, hon... and names Northern Food I/E Inc. as the recalling firm. Use the source fields below to narrow the match, then verify the exact item and current remedy on the issuing-agency page.

  • Firm: Northern Food I/E Inc.
  • Classification: Class I
  • Status: Terminated
  • Recall date: 2022-12-05
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Product Description & Identification

"Lukai sweetened jujube"; 8.3 ounces; red and yellow packaging; back panel states: "Name: Ejiao dates; Ingredients: a nuclear-free golden jujube, donkey-hide gelatin, sugar, honey, maltose, citric acid; Consumption methods: open bags of ready-to-eat, soup, making cakes; Shelf life: 12 months; Place of Origin: China Chengdu; Storage: Please store in a dry well-ventilated place, or frozen better; American General Agency: NORTHERN FOOD I/E INC"

Reason for Recall / Hazard Identified

Product contains undeclared sulfites (17.9mg/serving).

How to Check Whether Your Product Matches

A matching product name or photograph is not enough by itself. Compare every identifier available on your item or packaging with the official notice.

  1. Confirm the full product and brand or recalling-firm name.
  2. Compare package size, color, flavor, model, style, or configuration when listed.
  3. Check UPC, lot, batch, serial, date code, recall number, or USDA establishment number.
  4. Review the recall date and distribution information without assuming every seller is listed.
  5. Open the official FDA source below and follow its current instructions.

If a required identifier is missing, contact the recalling company or issuing agency through the official notice rather than guessing.

Consumer Action Recorded in the Source

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Distribution & Affected States

AL, CA, CT, FL, GA, IL, IN, LA, NY, NJ, OH, PA, TX

Verify With the Issuing Agency

This record was last updated in our index on 2026-08-09 21:59:13 UTC. Because recall enforcement statuses and instructions evolve, always verify details directly with the issuing government agency.

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Record Transparency

Issuing agency
FDA
Source ID
F-0212-2023
Indexed update
2026-08-09 21:59:13 UTC
Official source
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